Medical Device Manufacturer · US , San Leandro , CA

Codonics, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1996

Recent clearances: CODONICS SAFE LABELING SYSTEM (SLS), MODEL 500I/500P, CODONICS HORIZON XL DIGITAL DIRECT LONG FILM IMAGER, NP-2600 SERIES HARDCOPY PRINTERS

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

Codonics, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Leandro, US.

Historical record: 7 cleared submissions from 1996 to 2011. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Codonics, Inc. Filter by specialty or product code using the sidebar.

Codonics, Inc. is one of 18376 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Codonics, Inc.

7 devices

1-7 of 7

Cleared Feb 07, 2011

CODONICS SAFE LABELING SYSTEM (SLS), MODEL 500I/500P

Anesthesiology · 259d

Cleared Mar 16, 2006

CODONICS HORIZON XL DIGITAL DIRECT LONG FILM IMAGER

Radiology · 23d

Cleared Oct 05, 2004

NP-2600 SERIES HARDCOPY PRINTERS

Radiology · 49d

Cleared Apr 30, 2003

CODONICS EP-1000 MEDICAL COLOR DRY IMAGERS

Radiology · 56d

Cleared May 09, 2002

CODONICS HORIZON CI MEDICAL MULTIMEDIA DRY IMAGER

Radiology · 38d

Cleared Jan 19, 2001

CODONICS NP-1660 SERIES MEDICAL PRINTERS, MODEL 1660

Radiology · 71d

Cleared Nov 08, 1996

CODONICS MEDICAL PRINTER (NP-1600M,NP1600MD)

Radiology · 142d